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. 2016 Apr 7;11(4):e0152660. doi: 10.1371/journal.pone.0152660

Disease Burden Due to Herpes Zoster among Population Aged ≥50 Years Old in China: A Community Based Retrospective Survey

Yan Li 1,#, Zhijie An 1,#, Dapeng Yin 1, Yanmin Liu 1, Zhuoying Huang 2, Jianfang Xu 3, Yujie Ma 4, Qiufeng Tu 5, Qi Li 6, Huaqing Wang 1,*
Editor: Graciela Andrei7
PMCID: PMC4824529  PMID: 27055179

Abstract

Objective

To understand the disease burden due to Herpes Zoster (HZ) among people aged ≥50 years old in China and provide baseline data for future similar studies, and provide evidence for development of herpes zoster vaccination strategy.

Methods

Retrospective cohort study was conducted in 4 townships and one community. A questionnaire was used to collect information on incidence and cost of HZ among people aged ≥ 50 years old.

Results

The cumulative incidence rate was 22.6/1,000 among people aged ≥ 50 years old. The average annual incidence rate of HZ was 3.43/1,000 among people aged ≥ 50 years old in 2010–2012. Cumulative incidence and average annual incidence rate increased with age: the cumulative incidence of HZ among people aged ≥ 80 years old was 3.34 times of that among 50- years old (52.3/1000vs15.7/1,000); average annual incidence rate rises from 2.66/1,000 among 50- years old to 8.55/1,000 among 80- year old. Cumulative incidence and average annual incidence rate for females were higher than that for males (cumulative incidence, 26.5/1000vs18.7/1,000; annual incidence rate, 3.95/1000vs2.89/1,000). Cumulative incidence and average annual incidence rate in urban were higher than in rural (cumulative incidence, 39.5/1000vs 17.2/1,000; annual incidence rate, 7.65/1000vs2.06/1,000). The hospitalization rate of HZ was 4.53%. And with the increase of age, the rate has an increasing trend. HZ costs 945,709.5 RMB in total, corresponding to 840.6 RMB per patient with a median cost of 385 RMB (interquartile range 171.7–795.6). Factors associated with cost included the first onset year, area, whether hospitalized and whether sequelae left.

Conclusion

Incidence rate, complications, hospitalization rate and average cost of HZ increase with age. We recommend that the HZ vaccinations should target people aged ≥50 years old if Zoster vaccine is licensed in China.

Introduction

Herpes zoster (HZ), a disease characterized by clusters of blisters along the areas innervated by sensory nerve, is caused by varicella-zoster virus (VZV). The disease is often accompanied by severe pain that negatively impact the quality of life. The incidence of HZ correlates with increasing age, especially people after 50 years old [12]. It is estimated that the risks of occurring HZ in people previously infected with varicella are 10%-30% and the severity also increases with age [37].The annual incidence of HZ in the year 2013, 2012 and 2011 in Guangdong, China was 5.8, 3.4 and 4.1 per 1000 person-years, respectively[8].

Zoster vaccine is an effective method to prevent HZ. A few countries have introduced the Zoster vaccine into the national immunization program since it was licensed. The Zoster vaccine was licensed for people at least 50 years of age who had not have prior HZ for the prevention of HZ in Australia and Europe, while target age is at least 60 years of age in the US [912]. There is rare surveillance data in China on HZ due to it is not a notifiable disease. In addition current available data in China are mostly focused on treatments, only one study [8] on epidemiology and incidence, and no data on economic burden is available, especially community and population based data.

Developing an effective immunization strategy against HZ should base on the baseline data, such as epidemiology of HZ in target population, incidence and cost of HZ etc. Therefore we conducted this community based, retrospective study with objectives to understand incidence and economic burden of HZ in selected communities among people aged ≥50 year olds, so as to provide rationale for evidence based immunization strategy for HZ vaccination in China, as well as to provide baseline data for future similar studies.

Materials and Methods

Study sites and subjects

One township from each province of Jiangsu, Heilongjiang, Jiangxi and Hebei (as representative of rural areas) was selected; and one community from Shanghai (as representative of urban areas) was selected to conduct the retrospective study. The study was conducted from May 2013 to May 2014, targeting people aged ≥50 years old who developed HZ prior to the study. This study was approved by the ethical review committee of Chinese center for disease control and prevention (the approve number: 201313). All subjects signed the informed consent before they were recruited in the survey.

Data collection and calculation of the incidence rate

Demographic information

Population register data from community residency committee (or village), or statistics from local public security department were used to collect demographic information for people aged ≥50 years old.

Case searching

We set up investigation team comprised of staff from local center for disease control and prevention, staff from local community health service center (or village doctors), and staff from community resident committees (or village committee). The team carried out a house to house census survey to collect HZ patient information, including all the self-reported HZ diagnosed by doctor. Thereafter the investigators carried out a face-to-face interview for the patients to collect detailed information on HZ disease.

Calculation of incidence rate

cumulative incidence rate=(number of people with prior HZ)÷(number of targeted people)×1000÷1000
Annual incidence rate=(number of people with HZ onset in a certain year)÷(number of targeted people)×1000÷1000

Data Collection Method and Contents

We conducted a face to face interview using a uniformed questionnaire to collect information on basic demographic information, clinical manifestations, treatment information and economic burden of HZ patients. The clinical manifestations, treatment information and the cost in hospital of patients from the urban area were mainly collected from health care records and the receipts of payments for medical treatment. The same information of outpatients who had an onset date within 2 years and all the inpatients from rural area was mainly collected via reviewing the hospital outpatient logs / inpatient records and the reimbursement records from New Rural Co-financing Medical System and the Health Care Insurance System. The information of the remaining outpatients from rural area as well as other expense of all patients were collected via the payment receipts and memory provided by the subjects.

Contents of basic demographic information

The basic information included gender, date of birth and location.

Contents of clinical manifestations

We collected the detailed clinical manifestations for the HZ occurred first time and the second recurrence, the information included the date of onset, age when HZ onset, duration of rash, locations of the herpes, how long the pain lasted, whether sequela occurred and the classification of the severity. If the HZ reoccurred more than two times, we didn’t collect the later manifestations and just asked how many times the HZ occurred for the same patient.

Contents of treatment information

Treatment information included the total numbers of outpatient visit, the hospital level of the first 3 visits, whether to hospitalize, if hospitalized, the hospital level of each hospitalization for the first 3 times, the total days of hospitalization, the course and the outcome of HZ.

Contents and calculation of the cost

Contents of cost data: Cost information included: 1) outpatient expenses; 2) hospitalization expenses; and 3) other expenses which include the cost of Over-The-Counter Drug, transportation cost due to seek medical service, productivity loss (caring for the patient), and other costs considered to be associated with the disease.

Discount rate: The discount rate was used to adjust the cost in variable years. Consumer Price Indices (CPI), obtained from the website of China National Bureau of Statistics from 1951 to 2013 in China, was used to calculate the annual average discount rate as follows [13].

Discount rate=(year=19512013CPI)÷(N+1)1=0.036

N = 2013–1951 = 62, the average discount rate was 0.036, we used 0.04 as the average discount rate in this study.

Conversion of cost in different years: Based on the price of 2013, the cost occurred in other years is converted into 2013 price.

year specific cost=(cost  in  ​ 2013)÷(1+discount  rate)(N-1)
N=2013onset year

Statistical method

EPI Data 3.1 was used to set up database, and double data entry was used to guarantee the quality. Statistical Product and Service Solution (SPSS version 17.0) was used for data analysis. Chi square was used to test qualitative data, with relative risk (RR) and 95% confidence interval (95%CI) calculated. ANOVA, t test and multiple linear regression were used to test quantitative data. First type error level was set to be 0.05.

Results

Incidence of HZ

The total target subjects aged ≥50 years old in study areas were 49,721 in our study, and 1126 people had developed HZ, the cumulative incidence rate was 22.6/1,000. Cumulative incidence increased with age, the highest incidence was among people aged ≥ 80 years old which was3.34 times higher than that among people aged 50- years old (52.3/1000vs 15.7/1,000). There were 461 male patients and 665 female patients with a male to female ratio of 1:1.44. Cumulative incidence rate in female was higher than that in male (26.5/1000 vs. 18.7/1,000, RR = 1.41, 95% CI = 1.26–1.59). There were 648 patients in rural areas, and 478 in urban areas. Cumulative incidence rate was higher in urban areas than that in rural areas (39.5/1000 vs17.2 /1,000, RR = 2.29, 95%CI = 2.04–2.57) (Table 1).

Table 1. Cumulative incidence and epidemiological characteristics of HZ in people aged ≥50 years old.

Variable Population Patient Number Cumulative incidence (/1,000) RR 95%CI
Age group (years)
50- 21571 338 15.7 Ref -
60- 16896 389 23.0 1.47 1.27–1.70
70- 8135 236 29.0 1.85 1.57–2.18
80- 3119 163 52.3 3.34 2.78–4.01
Gender
Male 24598 461 18.7 Ref -
Female 25123 665 26.5 1.41 1.26–1.59
Area
Rural 37607 648 17.2 Ref -
Urban 12114 478 39.5 2.29 2.04–2.57
Total 49721 1126 22.6

There were 144, 159 and 208 HZ patients in 2010, 2011, 2012 respectively, with an incidence rate of 2.90/1,000, 3.20/1,000 and 4.18/1,000 among people aged ≥ 50 years old. The average annual incidence rate was 3.43/1,000 for year 2010–2012. During the three years, average age-specific incidence rate increased with age, from 2.66/1,000 in 50- years old to 8.55/1,000 in 80- years old. Average annual incidence rate was higher in female than in male (3.95/1000 vs 2.89/1,000) and higher in urban areas than in rural areas (7.65/1000 vs 2.06/1,000) (Table 2).

Table 2. Incidence rate (/1,000) of HZ among people aged ≥ 50 years old from 2010 to 2012.

Variable Population 2010 2011 2012 Mean annual incidence rate
Patient Number Incidence rate Patient Number Incidence rate Patient Number Incidence rate
Age group (years)
50- 21571 37 1.72 66 3.06 69 3.20 2.66
60- 16896 54 3.20 41 2.43 70 4.14 3.26
70- 8135 26 3.20 33 4.06 35 4.30 3.85
80- 3119 27 8.66 19 6.09 34 10.90 8.55
Gender
Male 24598 63 2.56 60 2.44 90 3.66 2.89
Female 25123 81 3.22 99 3.94 118 4.70 3.95
Area
Rural 37607 61 1.62 81 2.15 91 2.42 2.06
Urban 12114 83 6.85 78 6.44 117 9.66 7.65
Total 49721 144 2.90 159 3.20 208 4.18 3.43

Characteristics of HZ

First onset age

In total 1,125 patients out of 1,126 reported the age of first onset, with the median age of 59 years old and interquartile of 52–68 years old. Cumulative incidence rate of HZ before 50 years old was 3.5/1,000, and increased with age, to 8.0/1,000, 10.7/1,000, 14.4/1,000 and 27.6/1,000 for 50-, 60-, 70-, and 80- years old age respectively (Table 3).

Table 3. Cases and cumulative incidence rates of HZ according to first onset age in people aged ≥ 50 years old.
First Onset age* Patient Number Cumulative Incidence Rates (/1,000)
50- 60- 70- 80- Sub-total 50- 60- 70- 80- Sub-total
<50 107 44 13 11 175 5.0 2.6 1.6 3.5 3.5
50- 231 141 21 7 400 10.7 8.3 2.6 2.2 8.0
60- 204 92 6 302 12.1 11.3 1.9 10.7
70- - 109 53 162 13.4 17.0 14.4
80- - - 86 86 27.6 27.6

* One patient didn’t report onset time.

Sequelae occurrence

About 16.6% (187/1,126) of HZ had sequelae left after HZ, including neuralgia (182), followed by erythema (15), papulovesicle (9), and blister (4), etc. The frequency of sequelae increased with age (Table 4).

Table 4. Age specific sequelae occurrence in HZ patients aged ≥ 50 years old.
Onset age* Patient Number Patientswith sequelae Percentage (%) Trends χ2 P
<50 175 27 15.4 8.486 0.0036
50- 400 54 13.5
60- 302 48 15.9
70- 162 36 22.2
80- 86 22 25.6
Total 1126 187 16.6

* One patient didn’t report onset time.

Recurrence

On average 2.8% (32/1,126) of HZ reported a second recurrence, 0.2% (2/1126) reported a third recurrence. No patients reported more than 3 times of recurrence.

Hospitalization rate of HZ

In total 4.53% (51/1,126) of HZ were admitted into hospital for treatments. The average length of hospital stay was 10 days (range: 3–51 days), with a median of 12.7 days based on 50 patients with complete information. There was statistical difference in hospitalization rates among gender and area: the rate for male higher than that for female, and higher in rural than that in urban. (Table 5).

Table 5. Hospitalization rates among HZ patients aged ≥ 50 years old and associated factors: logistic regression analysis.

Variable Parameter estimation Standard error Wald-Chi-Square P OR 95%CI
Age 0.1688 0.3138 0.2894 0.5906 1.184 0.640–2.190
First Onset age 0.1957 0.3040 0.4146 0.5197 1.216 0.670–2.207
First onset year 0.4502 0.2878 2.4465 0.1178 1.569 0.892–2.758
Gender -0.7145 0.2947 5.8782 0.0153 0.489 0.275–0.872
Area 1.8687 0.4116 20.6135 <0.0001 6.480 2.892–14.517

Cost of HZ

Cost data were collected from 1,125 HZ patients with only 1 missing because the discount rate couldn’t be calculated resulting from his being unable to remember the onset date. The cost for outpatient was not available for 18 out of the 1,125 patients, and not available for 2 inpatients.

The total cost of enrolled HZ patients was 945,709.5 RMB, with a mean of 840.6 RMB per patient, and a median cost of 385 RMB (interquartile: 171.7–795.6) (Table 6). After log conversion, the univariate analysis showed that cost of HZ was related with area, first onset age, first onset year, hospitalization or not, and whether there were any sequelae (Table 7). Multivariate linear regression analysis found that the factors associated with the cost include first onset year, area, hospitalization or not, and whether there were any sequelae (Table 8).

Table 6. Cost of HZ among people aged ≥50 years old (RMB).

Variable Total cost Number of patients Average Median 25% percentile 75% percentile Minimum Maximum
Outpatient expenses 601997.5 1107# 543.8 336 135.2 649.6 0 13312
Hospitalization expenses 220618.5 49% 4502.4 3260.4 1161.7 5715 136.6 30000
Other expenses 123093.6 1125 109.4 0 0 16.6 0 4401
Total 945709.5 1125 840.6 385 171.7 795.6 0 30002

# Cost of outpatient was not available for 18 patients.

% Cost of inpatient was not available for 2 patients

Table 7. Cost of HZ among people aged ≥ 50 years old and associated factors (RMB): Univariate analysis.

Variable Number of patients Total cost Mean Log Mean F or t P
Area
Rural 647 519520.66 802.97 257.04 104.32 <0.0001
Urban 478 426188.87 891.61 588.84
Gender
Male 461 402035.08 872.09 363.08 0.18 0.6686
Female 664 543674.45 818.79 371.54
Age groups (years)
50- 338 227836.05 674.07 331.13 2.29 0.0773
60- 389 293567.79 754.67 346.74
70- 235 267454.04 1138.1 407.38
80- 163 156851.64 962.28 446.68
First Onset age
<50 175 110921.31 633.84 165.96 20.67 <0.0001
50- 400 270546.53 676.37 363.08
60- 302 276600.07 916.89 416.87
70- 162 213582.86 1318.41 562.34
80- 86 73758.77 857.66 537.03
First Onset year
<1990 71 26207.31 369.12 69.18 46.27 <0.0001
1990- 53 36286.74 684.66 208.93
2000- 375 324018.12 864.05 331.13
2010- 626 559197.36 893.29 478.63
Hospitalized
Yes 51 286358.83 5614.88 3890.45 179.39 <0.0001
No 1074 659350.7 613.92 323.59
Sequelae
Yes 185 226029.38 1221.78 660.69 7.54 <0.0001
No 940 499061.64 530.92 302.00

Table 8. Cost of HZ among people aged ≥ 50 years old and associated factors (RMB): Multivariate analysis.

Variable Parameter estimation Standard error t P
First Onset age 0.02780 0.01489 1.87 0.0622
First onset year 0.14725 0.02178 6.76 <0.0001
Sequelae -0.30710 0.04071 -7.54 <0.0001
Hospitalization -0.54296 0.07629 -7.12 <0.0001
Gender 0.05173 0.03080 1.68 0.0933
Area -0.27258 0.03427 -7.96 <0.0001

F = 56.06, P<0.0001; R2 = 0.2393, adjusted R2 = 0.2351

Discussion

HZ is a common viral disease, due to viruses reactivated when the VZV specific immunity declines [1415]. We found that cumulative incidence of HZ was 22.6/1,000 (17.2/1000 in rural areas and 39.5/1000 in urban areas) among people aged ≥50 years with an average annual incidence rate of 3.43 / 1,000 (2.06/1000 in rural areas and 7.65/1000 in urban areas), which is similar to that in Guangdong, China [8] and that in North America, Europe and Asia-Pacific (3-5/1000) [16]. The average annual incidence rate in urban areas reported by our study is similar to that in Taiwan (>8.36/1,000) [17], Australia (9.67/1,000) [18], The United States (8.46/1000) [19] and South Korea (10/1,000) [20]. Both cumulative incidence and annual incidence rate of HZ increased with age, possibly related to the decline in immunity with age, which is consistent with reported abroad [12, 2122]. We also found a higher cumulative incidence and annual incidence rate in female than that in male, consistent with some domestic and abroad studies [8,1920, 2226], although some studies [2728] reported a non-statistical difference in incidence between female and male. Therefore, further researches are needed to understand whether a difference between genders really exists and if so, the mechanisms. Cumulative incidence and annual incidences vary among different regions. We found a lower incidence in rural areas than that in urban areas, with contributors to be further clarified. We also found a similar recurrent rate of 3% (34/1126), similar to that reported by Jie Fang (2.72%)[29]; and a hospitalization rate of 4.53%, similar to reported in Taiwan (>4.14% among people aged ≥60 years old) [17], but lower to that in Guangdong, China [8].

This study showed that the mean cost per HZ case was 840.6 RMB, with a median of 385 RMB. The majority of cost was direct treatment cost related to outpatient (average of 543.8yuan) and hospitalization costs (average of 4502.4yuan). The indirect cost related HZ was relatively low. Cost was higher for inpatients than for outpatients, and higher for patients with sequelae than those without sequelae.

There were 338 million people aged ≥50 years old in China (183 million in rural areas, and 155 million in urban areas) according to census in 2010 [30]. Based on cumulative incidence rate of HZ in rural areas and urban areas, it is projected that there were 9.27 million people who had suffered from HZ aged ≥50 years old across China, with a total cost of 7.793 billion RMB. Based on the average annual incidence rate in rural China and urban China in 2010–2012, we estimate that there are 1.563 million new HZ cases every year with a total cost of about 1.314 billion RMB across China.

In addition to the direct economic burden caused by HZ, the quality of life of patients is negatively influenced due to the severe pain caused by the disease, with physical (e.g., fatigue, weight loss, insomnia), psychological (e.g., difficulty in concentrating, depression), social (e.g., decreased social activities, change of social role) and functional (e.g., dressing, mobilization) influenced. These effects are particularly severe for elderly patients with HZ [31]. In the US, the postherpetic neuralgia is the third common cause of chronic neuropathic pain [32]. Therefore, it is necessary to consider the impact of disease on the quality of life of the patients in addition to the direct economic burden when HZ immunization strategy is developed.

The age specific incidence rate, sequelae, hospitalization rate, average cost of HZ all increase with age, therefore vaccination targeting younger age groups would be the most cost effective. It is recommended that Zoster vaccine is used for people aged ≥60 years old in US [12], and it is recommended that the Zoster vaccine is indicated in people aged ≥50 years old in Australia [10] and in Europe [11]. Considering local epidemiology of HZ and immunization policy abroad, based on the immune response observed in vaccinees aged 50–59 years comparable to that observed in vaccinees 60 years or older [33], we recommend that the Zoster vaccine is used for people aged ≥50 years old when it is available in China in the future and the long term protection of the vaccination also should be monitored in order to determine if the potential booster dose is necessary.

There are a few limitations in this study: 1) Memory bias. In total 11.1% of the HZ occurred before 2000, resulting in less reliable incidence and cost due to the only information source is memory. 2) The data on mortality and fatality couldn’t be obtained because since the retrospective nature. 3) Study sites were not selected randomly and subjects recruited were people aged ≥ 50 years old, therefore the results can only represent the population aged ≥ 50 years old in selected sites and the generalization to the population aged ≥ 50 years old in other areas should be with caution. However, because the provinces selected are representative of east, middle and west China, and rural and urban areas were selected, this study can partly reflect the incidence and cost of HZ in people aged ≥ 50 years old. This study can provide baseline information for future studies with representative sampling methods.

Supporting Information

S1 Dataset. Minimum database.

(XLSX)

S1 File. Declaration of variables in minimum database.

(DOCX)

Acknowledgments

We gratefully acknowledge the health workers from Huangpu CDC, Danyang CDC, Ningan CDC, Guixi CDC, Cangxian CDC and their affiliate community health service centers or township hospitals who participated in the field investigation.

Data Availability

All relevant data are within the paper and its Supporting Information files.

Funding Statement

The article was funded by China 12th five-year national science and technology major projects (2012ZX10004-703). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

References

  • 1.Oxman MN, Levin MJ, Johnson GR, Schmader KE, Straus SE, Gelb LD, et al. A vaccine to prevent herpes zoster and postherpetic neuralgia in older adults[J]. N Engl J Med, 2005,352 (22):2271–2284. [DOI] [PubMed] [Google Scholar]
  • 2.Kim YJ, Lee CN, Lim C-Y, Jeon WS, Park YM. Population-Based Study of the Epidemiology of Herpes Zoster in Korea. Korean Med Sci 2014; 29: 1706–1710. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Hope-Simpson RE. The nature of herpes zoster: a long term study and a new hypothesis. Proc R Soc Med 1965; 58: 9–20. [PMC free article] [PubMed] [Google Scholar]
  • 4.Ragozzino MW, Melton LJ, Kurland LT, Chu CP, Perry OH. Population-based study of herpes zoster and its sequelae. Medicine (Baltimore) 1982; 61(5):310–6. [DOI] [PubMed] [Google Scholar]
  • 5.Brisson M, Edmunds WJ, Law B, Gay NJ, Walld R, Brownell M, et al. Epidemiology of varicella zoster virus infection in Canada and the United Kingdom. Epidemiol Infect 2001;127: 305–14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Thomas SL, Hall AJ. What does epidemiology tell us about risk factors for herpes zoster? Lancet Infect Dis 2004; 4:26–33. [DOI] [PubMed] [Google Scholar]
  • 7.Volpi A, Gross G, Hercogova J, Johnson RW. Current management of herpes zoster. The European view. Am J Clin Dermatol 2005; 6(5):317–25. [DOI] [PubMed] [Google Scholar]
  • 8.Zhu Q, Zheng H, Qu H, Deng H, Zhang J, Ma W, et al. Epidemiology of herpes zoster among adults aged 50 and above in Guangdong, China. Human Vaccines & Immunotherapeutics 11:8, 2113–2118. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Merck S&DA. ZOSTAVAX zoster virus vaccine live (Oka/Merck) MSD refrigerator stable (ZST/R-I-112007) Product Information. TGA approved September 12, 2007; Date of most recent ammendment January 7, 2008. Available from: URL: http://secure.healthlinks.net.au/content/csl/pi.cfm?product=cspzosta10708.
  • 10.Australian Technical Advisory Group on Immunisation (ATAGI). Systematic review of safety, immunogenicity and efficacy of zoster vaccines. Australian Government Department of Health and Ageing; 2008. Available from: URL:http://www.immunise.health.gov.au.
  • 11.Zostavax European Public Assessment Report; 2008 September 22.
  • 12.Harpaz R, Ortega-Sanchez I, Seward J. Prevention of herpes zoster: recommendations of the advisory committee on immunization practices (ACIP). MMWR 2008;57(5 (June 6)):1–30. [PubMed] [Google Scholar]
  • 13.http://data.stats.gov.cn/easyquery.htm?cn=C01. Access by May 15,2015.
  • 14.Feng XY, Wang FX. Herpes zoster neuralgia of the head and face [J].China Journal of Modern Medicine,2000, 10(12): 50. [Google Scholar]
  • 15.Fu-bin Wang. Analysis of 8 cases of chronic cholecystitis complicated with herpes zoster[J]. Chinese General Practice,2004, 7(20): 1493. [Google Scholar]
  • 16.Kawai Kosuke, Gebremeskel Berhanu G, Acosta Camilo J. Systematic review of incidence and complications of herpes zoster: towards a global perspective. BMJ Open 2014;4:e004833 10.1136/bmjopen-2014-004833 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Lin Y-H, Huang L-M, Chang I-S, Tsai F-Y, Lu C-Y, Shao P-L, et al. Disease burden and epidemiology of herpes zoster in pre-vaccine Taiwan[J]. Vaccine 28 (2010) 1217–1220. 10.1016/j.vaccine.2009.11.029 [DOI] [PubMed] [Google Scholar]
  • 18.Stein AN, Britt H, Harrison C, Conway EL, Anthony Cunningham, MacIntyre CR. Herpes zoster burden of illness and health care resource utilisation in the Australian population aged 50 years and older [J]. Vaccine 27 (2009) 520–529. 10.1016/j.vaccine.2008.11.012 [DOI] [PubMed] [Google Scholar]
  • 19.Johnson BH, Palmer L, Gatwood J, Lenhart G, Kawai K, Acosta CJ. Annual incidence rates of herpes zoster among an immunocompetent population in the United States. BMC Infectious Diseases (2015) 15:502 10.1186/s12879-015-1262-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Choi WS, Noh JY, Huh JY, Jo YM, Lee J, Song JY, et al. Disease burden of herpes zoster in Korea[J]. Journal of Clinical Virology 47 (2010) 325–329. 10.1016/j.jcv.2010.01.003 [DOI] [PubMed] [Google Scholar]
  • 21.Mullooly JP, Riedlinger K, Chun C, Weinmann S, Houston H. Incidence of herpes zoster, 1997–2002[J]. Epidemiol Infect, 2005, 133(2):245–253. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Pinchinat S, Cebrián-Cuenca AM, Bricout H, Johnson RW. Similar herpes zoster incidence across Europe: results from a systematic literature review. BMC Infectious Diseases 2013, 13:170 10.1186/1471-2334-13-170 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Opstelten W, Van Essen GA, Schellevis F, VERHEIJ THEO J.M., MOONS KAREL G.M.. Gender as an Independent risk factor for herpes zoster: a population-based prospective study[J]. Ann Epidemiol, 2006, 16(9):692–695. [DOI] [PubMed] [Google Scholar]
  • 24.Fleming DM, Cross KW, Cobb WA, Chapman RS. Gender difference in the incidence of shingles [J]. Epidemiol Infect,2004, 132 (1):1–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Jung HS, Kang JK, Yoo SH. Epidemiological Study on the Incidence of Herpes Zoster in Nearby Cheonan. Korean J Pain 2015; 28: 193–197. 10.3344/kjp.2015.28.3.193 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Takao Y, Miyazaki Y, Okeda M, Onishi F, Yano S, Gomi Y, et al. Incidences of Herpes Zoster and Postherpetic Neuralgia in Japanese Adults Aged 50 Years and Older From a Community-based Prospective Cohort Study: The SHEZ Study. J Epidemiol 2015; 25(10):617–625. 10.2188/jea.JE20140210 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Jung BF, Johnson RW, Griffin DR, Dworkin Robert H. Risk factors for postherpetic neuralgia in patients with herpes zoster [J]. Neurolo gy,2004, 62(9):1545–1551. [DOI] [PubMed] [Google Scholar]
  • 28.Scott FT, Leedham-Green ME, Barrett-Muir WY, Hawrami Khidir, Gallagher W Jane, Johnson Robert, et al. A study of shingles and the development of postherpetic neuralgia in East London [J]. J Med Virol, 2003,70 (Suppl 1):S24–S30. [DOI] [PubMed] [Google Scholar]
  • 29.Fang Jie, Yi-ping Lu, Xiao-chen Bao. A retrospective analysis of 184 cases of herpes zoster patients[J]. Journal of Liaoning University of Traditional Chinese Medicine, 2014, 16(3):177–178. [Google Scholar]
  • 30.China Statistics Press; Tabulation on the 2010 population census of the people’s republic of China (Book I):268–276. [Google Scholar]
  • 31.Schmader KE, Sloabe R, Pieper C, Coplan Paul M, Nikas Alexander, Saddier Patricia, et al. The impact of acute herpes zoster pain and discomfort on functional status and quality of life in older adults[J]. Clin J Pain, 2007. [DOI] [PubMed] [Google Scholar]
  • 32.Bennett GJ. Neuropathic pain: New insights, new interventions. Hosp Prac 33(1)95–144,1998. [DOI] [PubMed] [Google Scholar]
  • 33.PLOTKIN Stanley A., Orenstein Walter A., Offit Paul A.. Vaccines (6th edition):977. [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

S1 Dataset. Minimum database.

(XLSX)

S1 File. Declaration of variables in minimum database.

(DOCX)

Data Availability Statement

All relevant data are within the paper and its Supporting Information files.


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